A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909439



Internal ID22684649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119305765..119308410hg38UCSC Ensembl
chr10:121065277..121067922hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg382646
hg192646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367332
Samples
Known GenesGRK5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909439
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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